FDA UDI In Commercial Distribution 🇺🇸 United States

Meniett®

DI: 00721902935220 · Model: 1010020601 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Meniett®
Primary DI
00721902935220
Version / Model
1010020601
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-29
Public Version
3
Public Version Date
2019-03-04
Public Version Status
Update
Public Device Record Key
4776318b-9581-4922-bd2f-618232408ddc

Device Description

DEVICE 1010020601 MENIETT GENERATOR

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ETY TESTER, AUDITORY IMPEDANCE

GMDN Terms

Code Name
61904 Endolymph evacuator

Identifiers

Type ID
Primary 00721902935220

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K991562 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius